BRAIN

GRIN2A-related disorders: genotype and functional consequence predict phenotype

Tau PET in autosomal dominant Alzheimer’s disease: relationship with cognition, dementia and other biomarkers

Longitudinal multimodal MRI as prognostic and diagnostic biomarker in presymptomatic familial frontotemporal dementia

The bivariate distribution of amyloid-β and tau: relationship with established neurocognitive clinical syndromes

Prevention of tau seeding and propagation by immunotherapy with a central tau epitope antibody

Outcome prediction models in AQP4-IgG positive neuromyelitis optica spectrum disorders

Meningeal contribution to migraine pain: a magnetic resonance angiography study

MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1

Dysfunctional brain dynamics and their origin in Lewy body dementia

Proinflammatory CD20+ T cells in the pathogenesis of multiple sclerosis

Inhibition of EHMT1/2 rescues synaptic and cognitive functions for Alzheimer’s disease

Ossified blood vessels in primary familial brain calcification elicit a neurotoxic astrocyte response

The expanded clinical spectrum of anti-GABABR encephalitis and added value of KCTD16 autoantibodies

Brainstem spreading depolarization and cortical dynamics during fatal seizures in Cacna1a S218L mice

Cellular prion protein neither binds to alpha-synuclein oligomers nor mediates their detrimental effects

Reactivation of nonsense-mediated mRNA decay protects against C9orf72 dipeptide-repeat neurotoxicity

C9orf72 expansion within astrocytes reduces metabolic flexibility in amyotrophic lateral sclerosis

Frontal pathways in cognitive control: direct evidence from intraoperative stimulation and diffusion tractography

Polygenic hazard score, amyloid deposition and Alzheimer’s neurodegeneration

CD73-derived adenosine controls inflammation and neurodegeneration by modulating dopamine signalling

Brain vital signs detect concussion-related neurophysiological impairments in ice hockey

Loss of STEP61 couples disinhibition to N-methyl-d-aspartate receptor potentiation in rodent and human spinal pain processing

NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses

Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects

Interictal epileptiform discharges shape large-scale intercortical communication

The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations

Impaired forward model updating in young adults with Tourette syndrome

Type I interferon protects neurons from prions in in vivo models

Impaired reward-related learning signals in remitted unmedicated patients with recurrent depression

De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures

Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features

Long-range connections are more severely damaged and relevant for cognition in multiple sclerosis

Dorsal language stream anomalies in an inherited speech disorder

Traumatic axonal injury influences the cognitive effect of non-invasive brain stimulation

Theoretically meaningful models can answer clinically relevant questions

Holographic Display and Volumetric Light Sculpting by Dynamic Synthesis of 4d Light Fields

Artificial Intelligence, between Opportunity and Challenge

Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes

Reply: OnabotulinumtoxinA should be considered in medication overuse withdrawal in patients with chronic migraine

Recursive hierarchical embedding in vision is impaired by posterior middle temporal gyrus lesions

Grey Matter Leonardo da Vinci: a genius driven to distraction

Nervous Evaluation Conducted by the Changes of Ghrelin and Obestatin Executed by Aerobic Exercise

Imaging the behavior and neural activity of freely moving organisms with a gigapixel microscope

Holographic display for optical retinal prosthesis: design and validation

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2

High-Throughput Electrophysiological, Behavioral, or Social Event Triggered Imaging of Mouse Mesoscale Brain Activity

A New Method for Routing in Home Health Care Services